دورية أكاديمية
A novel approach to study multi-domain motions in JAK1’s activation mechanism based on energy landscape
| العنوان: | A novel approach to study multi-domain motions in JAK1’s activation mechanism based on energy landscape |
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| المؤلفون: | Sun, Shengjie, Rodriguez, Georgialina, Zhao, Gaoshu, Sanchez, Jason E, Guo, Wenhan, Du, Dan, Rodriguez Moncivais, Omar J, Hu, Dehua, Liu, Jing, Kirken, Robert Arthur, Li, Lin |
| المساهمون: | National Institutes of Health, National Institute on Minority Health and Health Disparities |
| المصدر: | Briefings in Bioinformatics ; volume 25, issue 2 ; ISSN 1467-5463 1477-4054 |
| بيانات النشر: | Oxford University Press (OUP) |
| سنة النشر: | 2024 |
| مصطلحات موضوعية: | Molecular Biology, Information Systems |
| الوصف: | The family of Janus Kinases (JAKs) associated with the JAK–signal transducers and activators of transcription signaling pathway plays a vital role in the regulation of various cellular processes. The conformational change of JAKs is the fundamental steps for activation, affecting multiple intracellular signaling pathways. However, the transitional process from inactive to active kinase is still a mystery. This study is aimed at investigating the electrostatic properties and transitional states of JAK1 to a fully activation to a catalytically active enzyme. To achieve this goal, structures of the inhibited/activated full-length JAK1 were modelled and the energies of JAK1 with Tyrosine Kinase (TK) domain at different positions were calculated, and Dijkstra’s method was applied to find the energetically smoothest path. Through a comparison of the energetically smoothest paths of kinase inactivating P733L and S703I mutations, an evaluation of the reasons why these mutations lead to negative or positive regulation of JAK1 are provided. Our energy analysis suggests that activation of JAK1 is thermodynamically spontaneous, with the inhibition resulting from an energy barrier at the initial steps of activation, specifically the release of the TK domain from the inhibited Four-point-one, Ezrin, Radixin, Moesin-PK cavity. Overall, this work provides insights into the potential pathway for TK translocation and the activation mechanism of JAK1. |
| نوع الوثيقة: | article in journal/newspaper |
| اللغة: | English |
| DOI: | 10.1093/bib/bbae079 |
| الإتاحة: | https://doi.org/10.1093/bib/bbae079Test https://academic.oup.com/bib/article-pdf/25/2/bbae079/56858794/bbae079.pdfTest |
| حقوق: | https://creativecommons.org/licenses/by/4.0Test/ |
| رقم الانضمام: | edsbas.966290EA |
| قاعدة البيانات: | BASE |
| DOI: | 10.1093/bib/bbae079 |
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